Suchergebnisse - "Nouri, Zahra"

PubPharm (53)

1

Axonal degeneration serum markers and temporal lobe atrophy in Alzheimer’s dementia continuum: a longitudinal study of plasma neurofilament light and tensor-based morphometry

enthalten in: bioRxiv.org | 2024

von Khodadadi, A. | Amirkhani, N. | Nouri, Z. | +5

2

Enhanced Induction of Apoptosis and Cell Cycle Arrest in MCF-7 Breast Cancer and HT-29 Colon Cancer Cell Lines via Low-Dose Biosynthesis of Selenium Nanoparticles Utilizing Lactobacillus casei

enthalten in: Biological trace element research | 2024

von Haji Mehdi Nouri, Z. | Tafvizi, F. | Amini, K. | +2

3

A novel METTL5 variant disrupting a donor splice site leads to primary microcephaly-related intellectual disability in an Iranian family: clinical features and literature review

enthalten in: Journal of genetics | 2023

von Shakarami, F. | Nouri, Z. | Khanahmad, H. | +2

4

A novel METTL5 variant disrupting a donor splice site leads to primary microcephaly-related intellectual disability in an Iranian family: clinical features and literature review

enthalten in: Journal of Genetics | 2023

von Shakarami, F. | Nouri, Z. | Khanahmad, H. | +2

5

Exploring Connections between Oral Microbiota, Short-Chain Fatty Acids, and Specific Cancer Types : A Study of Oral Cancer, Head and Neck Cancer, Pancreatic Cancer, and Gastric Cancer

enthalten in: Cancers | 2023

von Nouri, Z. | Choi, S. | Choi, I. | +13

6

A novel METTL5 variant disrupting a donor splice site leads to primary microcephaly-related intellectual disability in an Iranian family : clinical features and literature review

enthalten in: Journal of genetics | 2023

von Shakarami, F. | Nouri, Z. | Khanahmad, H. | +2

7

Novel in-frame duplication variant characterization in late infantile metachromatic leukodystrophy using whole-exome sequencing and molecular dynamics simulation

enthalten in: PloS one | 2023

von Ataei, Z. | Nouri, Z. | Tavakoli, F. | +3

8

X-linked mental retardation-hypotonic facies syndrome : Exome sequencing identifies novel clinical characteristics associated with c.5182G>C mutation in the ATRX gene

enthalten in: Molecular genetics & genomic medicine | 2022

von Shakarami, F. | Jahani, M. | Nouri, Z. | +1

9

Whole exome sequencing identified a novel LAMA2 frameshift variant causing merosin-deficient congenital muscular dystrophy in a patient with cardiomyopathy, and autism-like behavior

enthalten in: Neuromuscular disorders : NMD | 2022

von Nouri, Z. | Sarmadi, A. | Narrei, S. | +2

10

The microbiota-gut-kidney axis mediates host osmoregulation in a small desert mammal

enthalten in: NPJ biofilms and microbiomes | 2022

von Nouri, Z. | Zhang, X. | Khakisahneh, S. | +2

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